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rs397516232

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516232(C;T)
Make rs397516232(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23416057
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516232
ebirs397516232
HLIrs397516232
Exacrs397516232
Varsomers397516232
Maprs397516232
PheGenIrs397516232
hapmaprs397516232
1000 genomesrs397516232
hgdprs397516232
ensemblrs397516232
gopubmedrs397516232
geneviewrs397516232
scholarrs397516232
googlers397516232
pharmgkbrs397516232
gwascentralrs397516232
openSNPrs397516232
23andMers397516232
23andMe allrs397516232
SNP Nexus

SNPshotrs397516232
SNPdbers397516232
MSV3drs397516232
GWAS Ctlgrs397516232
Max Magnitude0
ClinVar
Risk rs397516232(T;T)
Alt rs397516232(T;T)
Reference rs397516232(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7 MHRT
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23885266G>A
CLNSRC ClinVar
CLNACC RCV000035937.4,